Remifentanil as pain relief during labour
- Conditions
- abour pain
- Registration Number
- EUCTR2005-004577-23-NO
- Lead Sponsor
- niversitetet i Bergen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
Healthy primiparaous woman with a normal pregnancy coming to full term labour, wishing pain relief to stand the labour pain.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Abnormal pregnancy or labour (Hypertension, bleeding disturbances, pregnancy intoxication, multiple foetous, abnormal foetus)
Any other opioid given within the 8 last hours before study start
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method